Novum Pharmaceutical Research Services is a global company that values teamwork and a commitment to excellence. The Project Manager will oversee day-to-day clinical trial activities for late phase assigned trials, ensuring adherence to protocols and regulatory standards while managing timelines and budgets.
Responsibilities:
- Manage assigned projects from the development of the protocol through production of the final report, included, but not limited to, the following:
- Identify and select Investigator Sites
- Negotiate Investigator agreements and ensure timely payment of Investigator Sites
- Manage projects to ensure timelines and budget are met
- Train team members on assigned study
- Write final report text and collaborate with statisticians, report writer, medical personnel, and Scientific Affairs to product final study report
- Review monitoring reports
- Supervise monitoring staff during project
- Communicate study status to senior management and sponsors
Requirements:
- Bachelor's degree (B.S.) and one-year experience as CRO Project Manager, preferably in oncology and/or equivalent combination of training and education
- Experience in clinical documentation supporting regulatory submissions
- Ability to travel 25% that will be irregular in nature and may include international travel
- Valid Driver's License
- CRO Project Manager: 2 years (Required)
- Willingness to travel: 25% (Required)